Nephros, Inc.

Nephros, Inc. — FDA 510(k) Submissions

Nephros, Inc. has submitted 8 FDA 510(k) premarket notifications since 2005, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Subsystem, Water Purification, System, Water Purification, General Medical Use, Dialyzer, High Permeability With Or Without Sealed Dialysate System . Use the specialty filter in the sidebar to narrow results.